ISO 22000 is an international food safety standard that is globally recognized and valid worldwide. A company within the food supply chain that applies and achieves ISO 22000 certification is regarded as having a well-established food safety management system and being capable of providing safe, high-quality food products to consumers.

ISO 22000 certification is a standard developed by the International Organization for Standardization (ISO) in the field of food safety.

ISO 22000:2018 certification is developed by the International Organization for Standardization (ISO) in the field of food safety. Implementing a food safety management system certification is considered a strategic and appropriate approach for organizations to improve overall food safety performance.

On June 19, 2018, the International Organization for Standardization (ISO) issued the new version of ISO 22000:2018 certification – Food Safety Management System.

SA 8000 is a social standard developed by Social Accountability International (SAI) to improve working conditions for employees in enterprises, farms, or offices. The standard is developed and overseen by Social Accountability International (SAI).

ISO 14001:2015 Certification – Environmental Management System is developed to establish a management system that helps agencies, organizations, and enterprises minimize negative environmental impacts arising from their business and production activities.

ISO 14001 helps enterprises minimize pollution risks, optimize resource use, improve operational efficiency, and gain competitive advantages in the green development trend. Explore the outstanding benefits of ISO 14001 together with the ISSQ Institute for Standard and Quality Development Studies.

ISO 14001:2015 certification is a set of environmental management standards developed to identify, manage, and control environmental aspects related to industrial and commercial activities.

ISO 14001:2015 is part of a set of international standards related to environmental management applicable to all organizations and enterprises anywhere. Built on the Plan – Do – Check – Act (PDCA) principle, ISO 14001:2015 specifies the most important requirements for identifying, controlling, and monitoring environmental aspects of organizations and enterprises, including methods for managing and improving the entire system.

Medical devices and instruments play an especially important role in medical examination and treatment and have a direct impact on human life and health. Products in this field must not only meet manufacturers’ standards but also comply with regulatory requirements to ensure that medical devices supplied to the market always meet quality and safety requirements for users.

ISO 13485 is a standard for safety management systems for medical products within the ISO 13485:2003 standards series issued by the International Organization for Standardization (ISO).

ISO 13485:2016 certification – the Medical Device Safety Management System has been widely accepted and applied by medical device manufacturers worldwide. These requirements are essential at present if organizations producing medical instruments, medical supplies, and medical devices wish their products to be recognized globally.